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rs794727290

From SNPedia

Orientationminus
Make rs794727290(-;-)
Make rs794727290(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position49430273
GeneDYM
is asnp
is mentioned by
dbSNPrs794727290
ebirs794727290
HLIrs794727290
Exacrs794727290
Varsomers794727290
Maprs794727290
PheGenIrs794727290
hapmaprs794727290
1000 genomesrs794727290
hgdprs794727290
ensemblrs794727290
gopubmedrs794727290
geneviewrs794727290
scholarrs794727290
googlers794727290
pharmgkbrs794727290
gwascentralrs794727290
openSNPrs794727290
23andMers794727290
23andMe allrs794727290
SNP Nexus

SNPshotrs794727290
SNPdbers794727290
MSV3drs794727290
GWAS Ctlgrs794727290
Max Magnitude
ClinVar
Risk rs794727290(;)
Alt rs794727290(;)
Reference rs794727290(T;T)
Significance Pathogenic
Disease Dyggve-Melchior-Clausen syndrome Smith McCort dysplasia
Variation info
Gene DYM
CLNDBN Dyggve-Melchior-Clausen syndrome Smith McCort dysplasia
Reversed 1
HGVS NC_000018.9:g.46956643delA
CLNSRC
CLNACC RCV000175879.1, RCV000175880.1,